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1-butyl-3-hydroxy-3-phenylindolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136369-01-2

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136369-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136369-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136369-01:
(8*1)+(7*3)+(6*6)+(5*3)+(4*6)+(3*9)+(2*0)+(1*1)=132
132 % 10 = 2
So 136369-01-2 is a valid CAS Registry Number.

136369-01-2Downstream Products

136369-01-2Relevant academic research and scientific papers

Axial tri-tert-butylphosphane coordination to Rh2(OAc)4: Synthesis, structure, and catalytic studies

Tan, Jiantao,Kuang, Yi,Wang, Yi,Huang, Qingfei,Zhu, Jin,Wang, Yuanhua

, p. 3139 - 3147 (2016)

The introduction of strong σ-donor axial ligands to the Rh-Rh metal bond has been utilized as an effective way to provide new chemical reactivities to bimetallic dirhodium(II) complexes. In this report, Rh2(OAc)4 complexes with axial

Copper-catalyzed arylation of indolin-2,3-ones with arylboronic acids

Zhang, Jilei,Chen, Jiuxi,Ding, Jinchang,Liu, Miaochang,Wu, Huayue

supporting information; experimental part, p. 9347 - 9351 (2011/12/14)

A convenient and efficient Cu(OTf)2-catalyzed arylation of indolin-2,3-ones with arylboronic acids using cheap 1,10-phenanthroline hydrate as ligand was developed under air atmosphere, achieving 3-aryl-3-hydroxy-2- oxindoles in good to excellen

Synthesis of 3-Hydroperoxyindolin-2-ones and Oxidation of Sulphides to Sulphoxides by 3-Hyxdroperoxyindolin-2-ones

Nishio, Takehiko

, p. 1717 - 1720 (2007/10/02)

The 3-hydroperoxyindolin-2-ones 2 were prepared in moderate yields by the dye-sensitized photooxidation of the indolin-2-ones 1.The 3-hydroperoxyindolin-2-ones thus obtained oxidized a series of sulphides 4 selectively to the corresponding sulphoxides 5 without further oxidation to the sulphone.

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